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Shantel M. Weinsheimer, Ph.D. - Publications

Affiliations: 
2006 Wayne State University, Detroit, MI, United States 
Area:
Genetics, Molecular Biology
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20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Weinsheimer SM, Alexander MD, Nelson J, Cooke DL, Hetts SW, McCulloch CE, Kim H, Ko NU. Abstract P42: Genetic Variants Associated With Vasospasm Following Aneurysmal Subarachnoid Hemorrhage Stroke. 52. DOI: 10.1161/STR.52.SUPPL_1.P42  0.342
2019 Starnawska A, Hansen C, Sparsø T, Mazin W, Olsen L, Bertalan M, Buil A, Bybjerg-Grauholm J, Bækvad-Hansen M, Hougaard D, Mortensen PB, Pedersen CB, Nyegaard M, Werge T, Weinsheimer S. Differential Dna Methylation At Birth Associated With Mental Disorder In Individuals With 22Q11.2 Deletion Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.245  0.31
2019 Weinsheimer S, Starnawska A, Hansen C, Buil A, Bybjerg-Grauholm J, Bækvad-Hansen M, Hougaard D, Sparsø T, Bertalan M, Mortensen PB, Pedersen CB, Werge T. Genome-Wide Methylomic Analysis Of Neonatal Blood From Danish Twins Discordant For Mental Illness European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.026  0.315
2018 Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Weinsheimer SM, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3  0.332
2018 Nelson J, Bendjilali N, Weinsheimer SM, McCulloch CE, Ko NU, Zaroff JG, Lawton MT, Pawlikowska L, Kim H. Abstract WP426: Does Intracerebral Hemorrhage in Brain Arteriovenous Malformation Share Genetic Risk Factors With Primary Intracerebral Hemorrhage? Stroke. 49. DOI: 10.1161/Str.49.Suppl_1.Wp426  0.334
2017 Starnawska A, Hansen CS, Sparsø T, Mazin W, Olsen L, Bertalan M, Buil A, Bybjerg-Grauholm J, Bækvad-Hansen M, Hougaard DM, Mortensen PB, Pedersen CB, Nyegaard M, Werge T, Weinsheimer S. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome. Translational Psychiatry. 7. PMID 28850114 DOI: 10.1038/Tp.2017.181  0.309
2016 Weinsheimer S, Bendjilali N, Nelson J, Guo DE, Zaroff JG, Sidney S, McCulloch CE, Al-Shahi Salman R, Berg JN, Koeleman BP, Simon M, Bostroem A, Fontanella M, Sturiale CL, Pola R, et al. Genome-wide association study of sporadic brain arteriovenous malformations. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 26818729 DOI: 10.1136/Jnnp-2015-312272  0.398
2015 Kremer PH, Koeleman BP, Pawlikowska L, Weinsheimer S, Bendjilali N, Sidney S, Zaroff JG, Rinkel GJ, van den Berg LH, Ruigrok YM, de Kort GA, Veldink JH, Kim H, Klijn CJ. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 524-9. PMID 25053769 DOI: 10.1136/Jnnp-2013-307276  0.468
2014 Tromp G, Weinsheimer S, Ronkainen A, Kuivaniemi H. Molecular basis and genetic predisposition to intracranial aneurysm. Annals of Medicine. 46: 597-606. PMID 25117779 DOI: 10.3109/07853890.2014.949299  0.571
2014 Bendjilali N, Nelson J, Weinsheimer S, Sidney S, Zaroff JG, Hetts SW, Segal M, Pawlikowska L, McCulloch CE, Young WL, Kim H. Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 1280-3. PMID 24777168 DOI: 10.1136/Jnnp-2013-306461  0.443
2013 Bendjilali N, Kim H, Weinsheimer S, Guo DE, Kwok PY, Zaroff JG, Sidney S, Lawton MT, McCulloch CE, Koeleman BP, Klijn CJ, Young WL, Pawlikowska L. A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. Plos One. 8: e71434. PMID 24098321 DOI: 10.1371/Journal.Pone.0071434  0.388
2012 Weinsheimer S, Brettman AD, Pawlikowska L, Wu DC, Mancuso MR, Kuhnert F, Lawton MT, Sidney S, Zaroff JG, McCulloch CE, Young WL, Kuo C, Kim H. G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation. Translational Stroke Research. 3: 418-27. PMID 23329986 DOI: 10.1007/S12975-012-0202-9  0.381
2011 Weinsheimer SM, Xu H, Achrol AS, Stamova B, McCulloch CE, Pawlikowska L, Tian Y, Ko NU, Lawton MT, Steinberg GK, Chang SD, Jickling G, Ander BP, Kim H, Sharp FR, et al. Gene expression profiling of blood in brain arteriovenous malformation patients. Translational Stroke Research. 2: 575-87. PMID 22184505 DOI: 10.1007/S12975-011-0103-3  0.38
2011 Mikhak B, Weinsheimer S, Pawlikowska L, Poon A, Kwok PY, Lawton MT, Chen Y, Zaroff JG, Sidney S, McCulloch CE, Young WL, Kim H. Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations. Cerebrovascular Diseases (Basel, Switzerland). 31: 338-45. PMID 21212665 DOI: 10.1159/000322601  0.395
2009 Weinsheimer S, Kim H, Pawlikowska L, Chen Y, Lawton MT, Sidney S, Kwok PY, McCulloch CE, Young WL. EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. Circulation. Cardiovascular Genetics. 2: 476-82. PMID 20031623 DOI: 10.1161/Circgenetics.109.883595  0.429
2008 Helgadottir A, Thorleifsson G, Magnusson KP, Grétarsdottir S, Steinthorsdottir V, Manolescu A, Jones GT, Rinkel GJ, Blankensteijn JD, Ronkainen A, Jääskeläinen JE, Kyo Y, Lenk GM, Sakalihasan N, Kostulas K, ... ... Weinsheimer S, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nature Genetics. 40: 217-24. PMID 18176561 DOI: 10.1038/Ng.72  0.551
2007 Weinsheimer S, Lenk GM, van der Voet M, Land S, Ronkainen A, Alafuzoff I, Kuivaniemi H, Tromp G. Integration of expression profiles and genetic mapping data to identify candidate genes in intracranial aneurysm. Physiological Genomics. 32: 45-57. PMID 17878320 DOI: 10.1152/Physiolgenomics.00015.2007  0.532
2007 Weinsheimer S, Goddard KA, Parrado AR, Lu Q, Sinha M, Lebedeva ER, Ronkainen A, Niemelä M, Khusnutdinova EK, Khusainova RI, Helin K, Jääskeläinen JE, Sakovich VP, Land S, Kuivaniemi H, et al. Association of kallikrein gene polymorphisms with intracranial aneurysms. Stroke; a Journal of Cerebral Circulation. 38: 2670-6. PMID 17761919 DOI: 10.1161/Strokeaha.107.486225  0.551
2007 Lenk GM, Tromp G, Weinsheimer S, Gatalica Z, Berguer R, Kuivaniemi H. Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms. Bmc Genomics. 8: 237. PMID 17634102 DOI: 10.1186/1471-2164-8-237  0.553
2005 Fayz B, Moldenhauer JS, Wang D, Zhao C, Yao B, Liu D, Weinsheimer S, Gardner L, Johnson A, Womble DD, Krawetz SA. LARALink: A web application for cytogenetic linkage analysis Clinical Genetics. 67: 314-321. PMID 15733267 DOI: 10.1111/J.1399-0004.2005.00409.X  0.342
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